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CAS

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1384975-97-6

3-phenyl-10H-furo[2,3-a]carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384975-97-6 Structure

  • Basic information

    1. Product Name: 3-phenyl-10H-furo[2,3-a]carbazole
    2. Synonyms: 3-phenyl-10H-furo[2,3-a]carbazole
    3. CAS NO:1384975-97-6
    4. Molecular Formula:
    5. Molecular Weight: 283.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384975-97-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-phenyl-10H-furo[2,3-a]carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-phenyl-10H-furo[2,3-a]carbazole(1384975-97-6)
    11. EPA Substance Registry System: 3-phenyl-10H-furo[2,3-a]carbazole(1384975-97-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1384975-97-6(Hazardous Substances Data)

1384975-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384975-97-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,9,7 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1384975-97:
(9*1)+(8*3)+(7*8)+(6*4)+(5*9)+(4*7)+(3*5)+(2*9)+(1*7)=226
226 % 10 = 6
So 1384975-97-6 is a valid CAS Registry Number.

1384975-97-6Downstream Products

1384975-97-6Relevant articles and documents

Facile synthesis of substituted furo-and pyrano-carbazoles

Prabakaran, Kumaresan,Prasad, Karnam Jayarampillai Rajendra

, p. 2966 - 2980 (2012/08/08)

Simple and efficient method for the synthesis of substituted furo-and pyrano-carbazole derivatives from 1-hydroxycarbazoles was described.

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